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An update on signal transduction and activator of transcription 3-hyper-IgE syndrome / 中华实用儿科临床杂志
Article in Zh | WPRIM | ID: wpr-990034
Responsible library: WPRO
ABSTRACT
Hyper-IgE syndrome (HIES) comprises a group of rare primary immunodeficiencies, which are characterized by extremely high serum IgE levels, eczema, recurrent skin and pulmonary infections.Signal transduction and activator of transcription 3( STAT3)-HIES is the most common type, which is caused by dominant-negative mutations in STAT3.STAT3-HIES confers broad innate and acquired immune defects, defects in skeletal, connective tissue, and vascular functions, causing a clinical phenotype including eczema, staphylococcal and fungal skin and pulmonary infections, scoliosis and minimal trauma fractures, vascular tortuosity and aneurysm.In this article, the advance in diverse clinical manifestations and management strategies of STAT3-HIES was summarized.
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Full text: 1 Index: WPRIM Language: Zh Journal: Chinese Journal of Applied Clinical Pediatrics Year: 2023 Type: Article
Full text: 1 Index: WPRIM Language: Zh Journal: Chinese Journal of Applied Clinical Pediatrics Year: 2023 Type: Article